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Zimmer Biomet, Inc. recalls Persona Partial Knee System Product Usage: The Persona Partial Knee System instruments are used by a surgeon to faci
Recalled February 21, 2018 · FDA recall Z-0596-2018 · Zimmer Biomet
Hazard
Potential for the Persona Partial Knee Impactor Pad to fracture. · FDA Class II
Units
1,275 units total
Sold at
US Nationwide Distribution in the states of AZ, CA, CO, ID, IL, IN, MA, MD, MI, NJ, NM, PA, SC, TX, WA, WI. Distributed internationally to Belgium, France, Germany, Italy, Japan, Netherlands, Spain, Sweden, Switzerland, UK.
Description
Potential for the Persona Partial Knee Impactor Pad to fracture.
Product
Persona Partial Knee System Product Usage: The Persona Partial Knee System instruments are used by a surgeon to facilitate the implantation of PPK implantable components into the medical knee compartment during unicondylar knee replacement.
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →